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甲状腺激素的组织特异性作用:来自动物模型的见解。

Tissue-specific actions of thyroid hormone: insights from animal models.

作者信息

Brent G A

机构信息

Molecular Endocrinology Laboratory, West Los Angeles VA Medical Center, Departments of Medicine and Physiology, UCLA School of Medicine, Los Angeles, CA, USA.

出版信息

Rev Endocr Metab Disord. 2000 Jan;1(1-2):27-33. doi: 10.1023/a:1010056202122.

Abstract

The major developmental targets for thyroid hormone are the brain, small intestine, and bone. Clear defects in gene regulation and tissue function as a consequence of TR gene inactivation can additionally be shown in the pituitary, hypothalamus, heart, and liver. TR gene knockout models show a clear distinction between thyroid hormone requirements for development and those that are required for functions in the adult animal. T3-mediated gene repression appears especially important in a number of tissues including brain, pituitary, and the heart. Preliminary evaluation of the combined TR knockout models suggests that hypothyroidism is associated with more significant abnormalities than receptor deficiency, indicating that the repressive action of the unliganded receptor may have physiological relevance. These various animal models should be very useful to design and test thyroid hormone analogues to selectively stimulate desired thyroid hormone actions.

摘要

甲状腺激素的主要发育靶点是脑、小肠和骨骼。TR基因失活导致的基因调控和组织功能明显缺陷,在垂体、下丘脑、心脏和肝脏中也有体现。TR基因敲除模型清楚地显示了成年动物发育所需的甲状腺激素与功能所需的甲状腺激素之间的区别。T3介导的基因抑制在包括脑、垂体和心脏在内的许多组织中似乎尤为重要。对联合TR敲除模型的初步评估表明,甲状腺功能减退比受体缺陷与更显著的异常有关,这表明未结合配体的受体的抑制作用可能具有生理相关性。这些不同的动物模型对于设计和测试甲状腺激素类似物以选择性地刺激所需的甲状腺激素作用应该非常有用。

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